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首页> 外文期刊>Angewandte Chemie >Polyfunctional Bis-Lewis-Acid-/Bis-Triazolium Catalysts for Stereoselective 1,4-Additions of 2-Oxindoles to Maleimides
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Polyfunctional Bis-Lewis-Acid-/Bis-Triazolium Catalysts for Stereoselective 1,4-Additions of 2-Oxindoles to Maleimides

机译:用于立体选择性1,4-二氧化二钒的多官能BIS-LEWIS-酸 - /双三唑催化剂

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摘要

Achieving enzyme-like catalytic activity and stereoselectivity without the typically high substrate specificity of enzymes is a challenge in the development of artificial catalysts for asymmetric synthesis. Polyfimctional catalysts are considered to be a promising tool for achieving excellent catalytic efficiency. A polyfunctional catalyst system was developed, which incorporates two Lewis acidic/BrOnsted basic cobalt centers in combination with triazolium moieties that are crucial for high reactivity and excellent stereoselectivity in the direct 1,4-addition of oxindoles to maleimides. The catalyst is assembled through click chemistry and is readily recyclable through precipitation by making use of its charges. Kinetic studies support a cooperative mode of action. Diastereodivergency is achievable with either Roc-protected or unprotected maleimide.
机译:在没有典型高衬底特异性的情况下实现酶样催化活性和立体选择性是在人工催化剂的不对称合成的发展中是一种挑战。 聚偏差催化剂被认为是实现优异的催化效率的有希望的工具。 开发了一种多官能催化剂体系,其含有两种Lewis酸性/伪装碱性钴中心,与三唑部分相结合,这对于高反应性和优异的立体选择性在直接1,4-加入马来酰亚胺中至关重要。 催化剂通过点击化学组装,通过使用其电荷来易于可回收沉淀。 动力学研究支持合作的行动方式。 诽谤率可与ROC保护或非保护的马来酰亚胺可实现。

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